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Variant (rsID / SNP)

rs259391

ADGB

rs259391 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADGB. Location: chromosome 6, position 147,106,841. The table records no clinical significance for this variant.

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Reference-table entries

ADGBNot classified
Variant type
synonymous_variant
Chromosome / position
6:147106841
HGVS
NM_024694.4,c.4308A>G,p.Lys1436Lys
Allele change
Synonymous_K1436K

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.